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prairie-willi

The I3PT wins 2 scholarships from the Ministry for a value of more than 700.000 euros
 The I3PT wins 2 scholarships from the Ministry for a value of more than 700.000 euros 1080 608 Oriol Capell
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The endowment will serve to finance the clinical trial of an innovative therapy for patients with Fragile X Syndrome and the discovery and clinical development of new PDE-10 inhibitors for the treatment of Prader-Willi syndrome read more
Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome
 Central adrenal insufficiency is rare in adults with Prader-Willi Syndrome 1080 675 Guillem Cebrian
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Prader-Willi syndrome (PWS) is a disease of uncommon genetic origin considered, however, the most common cause of genetic obesity. According to data extracted from the web portal of the Spanish SPW Association, this disease affects one in 15.000 newborns. A scientific article on this disease was recently published in The Journal of Clinical Endocrinology & Metabolism with the participation of several international researchers who are experts in this syndrome. Among them is Dr.…

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